Bartter and Gitelman's Syndromes Report

Dhs. 118.00

Bartter and Gitelman's Syndromes

Bartter and Gitelman's Syndromes are a spectrum of inherited tubulopathies sometimes difficult to distinguish, given the sharing of some characteristic metabolic abnormalities. These syndromes consist of impaired management of sodium, potassium and chloride in the renal tubules. Underlying genetic abnormalities impair the kidney's ability to reabsorb electrolytes, leading to typical signs and symptoms of the condition.

15 genes analyzed


It is recommended if:

This report is ideal for patients with a clinical suspicion of Bartter and Gitelman Syndromes.


List of main conditions:

  • Bartter syndrome, type 3
  • Bartter syndrome, type 5, antenatal, transient
  • Bartter syndrome, type 1
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • Investigates SNP and Indel mutations up to 150 bp

Simple workflow

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FAQs

How will my data be used?

Your data is yours. Which is why we have developed proprietary software linked to a dedicated platform, the Genome Manager, to provide you with unique access to your data whenever you want, wherever you are.

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You will be provided with a digital version of the raw data and reports. Thanks to these in-depth tools, you will be able to share your preferred information with your geneticist and/or doctor to indicate and plan the healthiest course for you. 

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